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Exceptionally fast temperature-responsive, mechanically strong and extensible monolithic non-porous hydrogels: poly(N-isopropylacrylamide) intercalated with hydroxypropyl methylcellulose

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    SYSNO ASEP0580772
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleExceptionally fast temperature-responsive, mechanically strong and extensible monolithic non-porous hydrogels: poly(N-isopropylacrylamide) intercalated with hydroxypropyl methylcellulose
    Author(s) Strachota, Beata (UMCH-V) RID
    Strachota, Adam (UMCH-V) RID, ORCID
    Vratović, Leana (UMCH-V)
    Pavlova, Ewa (UMCH-V) RID
    Šlouf, Miroslav (UMCH-V) RID, ORCID
    Kamel, S. (EG)
    Cimrová, Věra (UMCH-V) RID, ORCID
    Article number926
    Source TitleGels. - : MDPI
    Roč. 9, č. 12 (2023)
    Number of pages25 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordshydrogels ; drug release ; smart materials
    Subject RIVCD - Macromolecular Chemistry
    OECD categoryPolymer science
    Method of publishingOpen access
    Institutional supportUMCH-V - RVO:61389013
    UT WOS001131988500001
    EID SCOPUS85180715788
    DOI10.3390/gels9120926
    AnnotationExceptionally fast temperature-responsive, mechanically strong, tough and extensible monolithic non-porous hydrogels were synthesized. They are based on divinyl-crosslinked poly(N-isopropyl-acrylamide) (PNIPAm) intercalated by hydroxypropyl methylcellulose (HPMC). HPMC was largely extracted after polymerization, thus yielding a ‘template-modified’ PNIPAm network intercalated with a modest residue of HPMC. High contents of divinyl crosslinker and of HPMC caused a varying degree of micro-phase-separation in some products, but without detriment to mechanical or tensile properties. After extraction of non-fixed HPMC, the micro-phase-separated products combine superior mechanical properties with ultra-fast T-response (in 30 s). Their PNIPAm network was highly regular and extensible (intercalation effect), toughened by hydrogen bonds to HPMC, and interpenetrated by a network of nano-channels (left behind by extracted HPMC), which ensured the water transport rates needed for ultra-fast deswelling. Moreover, the T-response rate could be widely tuned by the degree of heterogeneity during synthesis. The fastest-responsive among our hydrogels could be of practical interest as soft actuators with very good mechanical properties (soft robotics), while the slower ones offer applications in drug delivery systems (as tested on the example of Theophylline), or in related biomedical engineering applications.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2024
    Electronic addresshttps://www.mdpi.com/2310-2861/9/12/926
Number of the records: 1  

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